Canonical Allele Identifier: PA211368
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135724
ClinVar RCV Id: RCV000148374 RCV000122809 RCV000587542 RCV001549270 RCV000493019 RCV003534364 RCV001157355 RCV003153406
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ile2756Val
CA014501
NM_000038.6:c.8266A>G